TY - JOUR
T1 - Integration of single-cell multi-omics for gene regulatory network inference
AU - Hu, Xinlin
AU - Hu, Yaohua
AU - Wu, Fanjie
AU - Leung, Ricky Wai Tak
AU - Qin, Jing
N1 - Funding Information:
This work was supported by the Natural Science Foundation of Guangdong Province of China (2019A1515011917, 2020B1515310008), Project of Educational Commission of Guangdong Province of China (2019KZDZX1007), Natural Science Foundation of Shenzhen (JCYJ20190808173603590, JCYJ20170817100950436, JCYJ20170818091621856) and Interdisciplinary Innovation Team of Shenzhen University. We would like to thank three anonymous reviewers and the editor for their constructive comments.
Funding Information:
This work was supported by the Natural Science Foundation of Guangdong Province of China ( 2019A1515011917 , 2020B1515310008 ), Project of Educational Commission of Guangdong Province of China ( 2019KZDZX1007 ), Natural Science Foundation of Shenzhen ( JCYJ20190808173603590 , JCYJ20170817100950436 , JCYJ20170818091621856 ) and Interdisciplinary Innovation Team of Shenzhen University . We would like to thank three anonymous reviewers and the editor for their constructive comments.
Publisher Copyright:
© 2020 The Authors
PY - 2020
Y1 - 2020
N2 - The advancement of single-cell sequencing technology in recent years has provided an opportunity to reconstruct gene regulatory networks (GRNs) with the data from thousands of single cells in one sample. This uncovers regulatory interactions in cells and speeds up the discoveries of regulatory mechanisms in diseases and biological processes. Therefore, more methods have been proposed to reconstruct GRNs using single-cell sequencing data. In this review, we introduce technologies for sequencing single-cell genome, transcriptome, and epigenome. At the same time, we present an overview of current GRN reconstruction strategies utilizing different single-cell sequencing data. Bioinformatics tools were grouped by their input data type and mathematical principles for reader's convenience, and the fundamental mathematics inherent in each group will be discussed. Furthermore, the adaptabilities and limitations of these different methods will also be summarized and compared, with the hope to facilitate researchers recognizing the most suitable tools for them.
AB - The advancement of single-cell sequencing technology in recent years has provided an opportunity to reconstruct gene regulatory networks (GRNs) with the data from thousands of single cells in one sample. This uncovers regulatory interactions in cells and speeds up the discoveries of regulatory mechanisms in diseases and biological processes. Therefore, more methods have been proposed to reconstruct GRNs using single-cell sequencing data. In this review, we introduce technologies for sequencing single-cell genome, transcriptome, and epigenome. At the same time, we present an overview of current GRN reconstruction strategies utilizing different single-cell sequencing data. Bioinformatics tools were grouped by their input data type and mathematical principles for reader's convenience, and the fundamental mathematics inherent in each group will be discussed. Furthermore, the adaptabilities and limitations of these different methods will also be summarized and compared, with the hope to facilitate researchers recognizing the most suitable tools for them.
KW - Gene regulatory network inference
KW - Single-cell multi-omics integration
KW - Single-cell sequencing
UR - http://www.scopus.com/inward/record.url?scp=85088369138&partnerID=8YFLogxK
U2 - 10.1016/j.csbj.2020.06.033
DO - 10.1016/j.csbj.2020.06.033
M3 - Review article
C2 - 32774787
AN - SCOPUS:85088369138
SN - 2001-0370
VL - 18
SP - 1925
EP - 1938
JO - Computational and Structural Biotechnology Journal
JF - Computational and Structural Biotechnology Journal
ER -